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662086 UCH-L1 Inhibitor - CAS 668467-91-2 - Calbiochem

662086
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
668467-91-2C₁₇H₁₁Cl₃N₂O₃

Products

产品目录编号包装 数量 / 包装
662086-10MGCN 玻璃瓶 10 mg
Description
OverviewAn isatin O-acyl oxime compound that acts as a potent, reversible, competitive, and active site-directed inhibitor of UCH-L1 (Ki = 0.40 µM; IC50 = 0.88 µM) with ~28-fold greater selectivity over UCH-L3 (Cat. No. 662090). Shown to increase proliferation of UCH-L1 expresssing tumor cell line SH-SY5Y at 5 µM. A useful tool for studying the roles of UCH-L1 in cancer, Parkinson’s disease, and other neurological disorders. Permeability may vary from cell type to cell type.
Catalogue Number662086
Brand Family Calbiochem®
SynonymsLDN-57444, Ubiquitin C-Terminal Hydrolase L1 Inhibitor, Ubiquitin C-Terminal Esterase L1 Inhibitor, Ubiquitin Thiolesterase L1 Inhibitor
References
ReferencesLiu, Y., et al. 2003. Chem. Biol. 10, 837.
Product Information
CAS number668467-91-2
ATP CompetitiveY
FormOrange solid
Hill FormulaC₁₇H₁₁Cl₃N₂O₃
Chemical formulaC₁₇H₁₁Cl₃N₂O₃
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetUCH-L1
Primary Target IC<sub>50</sub>0.88 µM
Primary Target K<sub>i</sub>0.40 µM
Purity≥95% by HPLC
Physicochemical Information
Cell permeableN
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Toxicity Carcinogenic / Teratogenic
Storage +2°C to +8°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
产品目录编号 GTIN
662086-10MGCN 04055977261134

Documentation

UCH-L1 Inhibitor - CAS 668467-91-2 - Calbiochem MSDS

职位

物料安全数据表 (MSDS) 

UCH-L1 Inhibitor - CAS 668467-91-2 - Calbiochem 分析证书

标题批号
662086

参考

参考信息概述
Liu, Y., et al. 2003. Chem. Biol. 10, 837.
数据表

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision19-April-2011 RFH
SynonymsLDN-57444, Ubiquitin C-Terminal Hydrolase L1 Inhibitor, Ubiquitin C-Terminal Esterase L1 Inhibitor, Ubiquitin Thiolesterase L1 Inhibitor
DescriptionA potent, reversible, competitive, and active site-directed inhibitor of ubiquitin C-terminal hydrolase L1 (UCH-L1) (Ki = 400 nM; IC50 = 880 nM). Exhibits ~28-fold greater selectivity for UCH-L1 compared to UCH-L3 (Cat. No. 662090). Shown to increase proliferation of the UCH-L1-expressing tumor cell line, SH-SY5Y, at a concentration of 5 µM. Useful tool for studying the roles of UCH-L1 in cancer, Parkinson's disease, and other neurological disorders. Cell-permeability is reported to vary from cell type to cell type.
FormOrange solid
Intert gas (Yes/No) Packaged under inert gas
CAS number668467-91-2
Chemical formulaC₁₇H₁₁Cl₃N₂O₃
Structure formulaStructure formula
Purity≥95% by HPLC
SolubilityDMSO (20 mg/ml)
Storage Protect from light
+2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity Carcinogenic / Teratogenic
ReferencesLiu, Y., et al. 2003. Chem. Biol. 10, 837.